甲基莲心碱脂质体的研制及其体外释药考察  被引量:2

Study on the Preparation and Drug Release of Neferine Liposomes in Vitro

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作  者:杨淑清[1] 

机构地区:[1]武汉大学人民医院药学部,武汉430060

出  处:《中国药师》2010年第9期1255-1257,共3页China Pharmacist

摘  要:目的:研制甲基莲心碱脂质体,并对其体外性质进行考察。方法:采用薄膜分散法制备脂质体,利用正交实验对其处方进行优化对其形态、粒径、包封率及释药等体外性质进行考察。结果:甲基莲心碱脂质体形态规整,平均粒径为(842.5±4.65)nm,平均包封率为(72.8±1.5)%体外释药遵循Higuchi方程:Q=30.78t_(1/2)-5.12,(R^2=0.995),具有明显的缓释效果。结论:优化得到甲基莲心碱脂质体的处方及制备工艺,为进一步体内研究奠定了基础。Objective: To study the preparation of neferine liposomes and drug release in vitro. Method: Neferine liposomes was prepared by film dispersion method. The formulation was screened by orthonogonal test and the appearance, mean size, encapsulation rate (ER%) and drug release in vitro were studied. Result: The shape of neferine liposomes was spherical with mean diameter of (842. 5 ±4. 65) nm and ER% of (72. 8 ± 1.5 ) %. Drug release rate was accorded with Higuchi equation of Q = 30. 78t1/2 - 5.12, ( R2 = 0. 995 ), showed significant sustained release property. Conclusion: The optimal formulation and preparation process of neferine liposomes was the basis of further study in vivo.

关 键 词:甲基莲心碱 脂质体 制备 体外释药 

分 类 号:R945[医药卫生—微生物与生化药学]

 

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